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TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells

TEX101, a germ cell-specific glycosyl-phosphatidylinositol (GPI)-anchored glycoprotein, is associated with Ly6k during spermatogenesis in testis. Although both Tex101(−/−) and Ly6k(−/−) mice can produce morphologically intact spermatozoa, both knockout mice show an infertile phenotype due to a disor...

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Autores principales: Endo, Shuichiro, Yoshitake, Hiroshi, Tsukamoto, Hiroki, Matsuura, Hideyuki, Kato, Ko, Sakuraba, Mayumi, Takamori, Kenji, Fujiwara, Hiroshi, Takeda, Satoru, Araki, Yoshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804279/
https://www.ncbi.nlm.nih.gov/pubmed/27005865
http://dx.doi.org/10.1038/srep23616
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author Endo, Shuichiro
Yoshitake, Hiroshi
Tsukamoto, Hiroki
Matsuura, Hideyuki
Kato, Ko
Sakuraba, Mayumi
Takamori, Kenji
Fujiwara, Hiroshi
Takeda, Satoru
Araki, Yoshihiko
author_facet Endo, Shuichiro
Yoshitake, Hiroshi
Tsukamoto, Hiroki
Matsuura, Hideyuki
Kato, Ko
Sakuraba, Mayumi
Takamori, Kenji
Fujiwara, Hiroshi
Takeda, Satoru
Araki, Yoshihiko
author_sort Endo, Shuichiro
collection PubMed
description TEX101, a germ cell-specific glycosyl-phosphatidylinositol (GPI)-anchored glycoprotein, is associated with Ly6k during spermatogenesis in testis. Although both Tex101(−/−) and Ly6k(−/−) mice can produce morphologically intact spermatozoa, both knockout mice show an infertile phenotype due to a disorder of spermatozoa to migrate into the oviduct. Since Ly6k specifically interacts with TEX101, complex formation of TEX101/Ly6k appears to be potentially important for functional sperm production. This study evaluated the fate of Ly6k in the presence or absence of TEX101 to explore the molecular interaction of both GPI-anchored proteins in seminiferous tubules. The present study showed that: 1) Although Ly6k mRNA was detected, the protein was present at very low levels in mature testes of Tex101(−/−) mice, 2) Ly6k mRNA level was within the normal range in Tex101(−/−) mice, 3) Ly6k mRNA was translated into a polypeptide in the testes of Tex101(+/+) and Tex101(−/−) mice, and 4) TEX101, as well as Ly6k, are co-factors that affect to molecular expression. These results indicate that both TEX101 and Ly6k contribute to the post-translational counterpart protein expression at the cell membrane. This mechanism may be important in maintaining the production of fertile spermatozoa during spermatogenesis.
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spelling pubmed-48042792016-03-23 TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells Endo, Shuichiro Yoshitake, Hiroshi Tsukamoto, Hiroki Matsuura, Hideyuki Kato, Ko Sakuraba, Mayumi Takamori, Kenji Fujiwara, Hiroshi Takeda, Satoru Araki, Yoshihiko Sci Rep Article TEX101, a germ cell-specific glycosyl-phosphatidylinositol (GPI)-anchored glycoprotein, is associated with Ly6k during spermatogenesis in testis. Although both Tex101(−/−) and Ly6k(−/−) mice can produce morphologically intact spermatozoa, both knockout mice show an infertile phenotype due to a disorder of spermatozoa to migrate into the oviduct. Since Ly6k specifically interacts with TEX101, complex formation of TEX101/Ly6k appears to be potentially important for functional sperm production. This study evaluated the fate of Ly6k in the presence or absence of TEX101 to explore the molecular interaction of both GPI-anchored proteins in seminiferous tubules. The present study showed that: 1) Although Ly6k mRNA was detected, the protein was present at very low levels in mature testes of Tex101(−/−) mice, 2) Ly6k mRNA level was within the normal range in Tex101(−/−) mice, 3) Ly6k mRNA was translated into a polypeptide in the testes of Tex101(+/+) and Tex101(−/−) mice, and 4) TEX101, as well as Ly6k, are co-factors that affect to molecular expression. These results indicate that both TEX101 and Ly6k contribute to the post-translational counterpart protein expression at the cell membrane. This mechanism may be important in maintaining the production of fertile spermatozoa during spermatogenesis. Nature Publishing Group 2016-03-23 /pmc/articles/PMC4804279/ /pubmed/27005865 http://dx.doi.org/10.1038/srep23616 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Endo, Shuichiro
Yoshitake, Hiroshi
Tsukamoto, Hiroki
Matsuura, Hideyuki
Kato, Ko
Sakuraba, Mayumi
Takamori, Kenji
Fujiwara, Hiroshi
Takeda, Satoru
Araki, Yoshihiko
TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title_full TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title_fullStr TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title_full_unstemmed TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title_short TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells
title_sort tex101, a glycoprotein essential for sperm fertility, is required for stable expression of ly6k on testicular germ cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804279/
https://www.ncbi.nlm.nih.gov/pubmed/27005865
http://dx.doi.org/10.1038/srep23616
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